- Merck & Co. (Rahway, NJ)
- Job DescriptionWe are seeking a highly skilled, technical and strategic Associate Principal Scientist of Digital & Data Technology with a strong background ... efficient management of data across the organization, including compliance with regulatory standards, and the optimization of laboratory operations and workflows via… more
- Merck & Co. (Boston, MA)
- Job Description Senior Principal Scientist , Precision Medicine, Immunology Precision Medicine is an integral part of our Immunology Therapeutic Area. To support ... concepts aligned with the Precision Medicine goals for relevant programs/assetsThe Senior Principal Scientist is responsible for maintaining a strong scientific… more
- Merck & Co. (Rahway, NJ)
- …process validation, second generation process development and authoring of regulatory submissions.-Under the general scientific and administrative direction of the ... next generation process development and characterization, process validation, and regulatory submission authoringIn this role, the successful candidate will be… more
- Merck & Co. (North Wales, PA)
- …span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.-Design and maintain statistical ... and systems and database expertise;US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development… more
- Merck & Co. (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The incumbent is responsible for… more
- Merck & Co. (Rahway, NJ)
- …colleagues while developing and expanding your career.The Senior Clinical Director (Sr. Principal Scientist ) has primary responsibility for the planning and ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.- Specifically, the Senior Director may be… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Principal Scientist ( Associate Director) is responsible for developing and implementing Regulatory ... with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead...projects and be accountable for the delivery of all regulatory milestones for assigned products through the product lifecycle.… more
- Charles River Laboratories (Ashland, OH)
- …Ensure scientific Integrity of studies, with minimal oversight. * Function as a Principal Investigator, Individual Scientist , and/or Project Scientist as ... a career that you can feel passionate about. **Job Summary** Serve as a scientist in the conduct of assigned nonclinical research studies of basic complexity, to… more
- Merck (Rahway, NJ)
- **Job Description** We are seeking a highly skilled, technical and strategic Associate Principal Scientist of Digital & Data Technology with a strong ... efficient management of data across the organization, including compliance with regulatory standards, and the optimization of laboratory operations and workflows via… more
- Merck (Rahway, NJ)
- **Job Description** We are currently seeking an exceptional individual for an Associate Principal Scientist position within the Supply Analytical Sciences ... supply. The individual will have a deep understanding of the global regulatory and business environment and the needs related to pharmaceutical drug substance… more
- Bristol Myers Squibb (Princeton, NJ)
- …track record of high-quality scientific publications in relevant fields For the Sr. Principal Scientist position, the starting compensation for this job is a ... oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external… more
- Merck (San Francisco, CA)
- **Job Description** **Senior Principal Scientist , Precision Medicine, Immunology** Precision Medicine is an integral part of our Immunology Therapeutic Area. To ... aligned with the Precision Medicine goals for relevant programs/assets The Senior Principal Scientist is responsible for maintaining a strong scientific fund… more
- Bristol Myers Squibb (Devens, MA)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position:** Principal Scientist , Manufacturing Technology (Process Transfer, Validation ... and Projects) **Location** : Devens, MA **Position Summary** The Principal Scientist is a subject matter expert...site procedures, and that processes are defined consistent with regulatory guidance. The role will also be responsible for… more
- Merck (Rahway, NJ)
- …process validation, second generation process development and authoring of regulatory submissions. Under the general scientific and administrative direction of ... next generation process development and characterization, process validation, and regulatory submission authoring **In this role, the successful candidate will… more
- Merck (North Wales, PA)
- …the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. + Design and maintain ... systems and database expertise; + US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development… more
- Merck (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. The incumbent is responsible for… more
- Amgen (Washington, DC)
- …us and transform the lives of patients while transforming your career. **Senior Principal Scientist - Global Diagnostic Development Lead** **What you will do** ... assay to marketed Diagnostic to support the clinical development strategy for regulatory approval and commercialization. As such, the Dx group works closely with… more
- Walmart (Bentonville, AR)
- …service operations and technology solutions for Finance, People, and the Associate Digital Experience. **About People.AI Team** The People.AI team is responsible ... intelligent experience within a chatbot or business application to enhance associate experience and productivity. You will design and build an intelligent… more
- Dartmouth Health (Lebanon, NH)
- …under the limited supervision of an experienced investigator, the Scientist contributes to both developing and established research programs. Responsibilities ... writing and authors publications in national scientific journals. 4. Acts as Principal Investigator. 5. Manages the collection and analysis of data for research… more
